Revel Score:
ENST00000325823
0.099
ENST00000447912
0.099
ENST00000396410 (MANE Select)
0.099
ENST00000450288
0.099
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.15036083C>G , CM000678.2:g.15036083C>G | GRCh38 |
| NC_000016.9:g.15129940C>G , CM000678.1:g.15129940C>G | GRCh37 |
| NC_000016.8:g.15037441C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396410.9:c.2175C>G MANE Select | ENSP00000379691.4:p.His725Gln | |
| ENST00000396410.8:c.2175C>G | ENSP00000379691.4:p.His725Gln | |
| ENST00000450288.3:c.1902C>G | ENSP00000391147.3:p.His634Gln | |
| ENST00000535621.6:c.1399+6027C>G | ENSP00000437835.2:n.1399+6027C>G | |
| ENST00000562119.5:c.*464C>G | ENSP00000455486.1:n.*464C>G | |
| ENST00000563679.5:c.2229C>G | ENSP00000454791.1:p.His743Gln | |
| ENST00000565986.1:n.557C>G | ||
| ENST00000569715.5:c.2094C>G | ENSP00000455070.1:p.His698Gln | |
| ENST00000570001.5:n.3224C>G | ||
| ENST00000627450.2:c.2091C>G | ENSP00000486662.1:p.His697Gln | |
| NM_001285444.1:c.2094C>G | NP_001272373.1:p.His698Gln | |
| NM_001285445.1:c.2091C>G | NP_001272374.1:p.His697Gln | |
| NM_001285447.1:c.2130C>G | NP_001272376.1:p.His710Gln | |
| NM_001285448.1:c.1902C>G | NP_001272377.1:p.His634Gln | |
| NM_001285449.1:c.1399+6027C>G | NP_001272378.1:n.1399+6027C>G | |
| NM_015027.3:c.2175C>G | NP_055842.2:p.His725Gln | |
| XM_005255173.1:c.2229C>G | XP_005255230.1:p.His743Gln | |
| XM_005255176.2:c.2130C>G | XP_005255233.1:p.His710Gln | |
| XM_006720865.2:c.2049C>G | XP_006720928.2:p.His683Gln | |
| NM_001324019.1:c.2172C>G | NP_001310948.1:p.His724Gln | |
| NM_001324020.1:c.1396+6027C>G | NP_001310949.1:n.1396+6027C>G | |
| NM_001324021.1:c.1318+6027C>G | NP_001310950.1:n.1318+6027C>G | |
| XM_005255176.3:c.2130C>G | XP_005255233.1:p.His710Gln | |
| XM_017023059.1:c.2130C>G | XP_016878548.1:p.His710Gln | |
| XM_017023060.1:c.2202C>G | XP_016878549.1:p.His734Gln | |
| XM_017023061.2:c.2130C>G | XP_016878550.1:p.His710Gln | |
| XM_017023062.1:c.2130C>G | XP_016878551.1:p.His710Gln | |
| XM_017023063.1:c.*68C>G | XP_016878552.1:n.*68C>G | |
| XM_017023064.1:c.2049C>G | XP_016878553.1:p.His683Gln | |
| XM_017023065.1:c.1354+6027C>G | XP_016878554.1:n.1354+6027C>G | |
| XM_024450194.1:c.1354+6027C>G | XP_024305962.1:n.1354+6027C>G | |
| XM_024450195.1:c.1453+6027C>G | XP_024305963.1:n.1453+6027C>G | |
| XM_024450196.1:c.1426+6027C>G | XP_024305964.1:n.1426+6027C>G | |
| XM_024450197.1:c.1273+6027C>G | XP_024305965.1:n.1273+6027C>G | |
| NM_001285444.2:c.2094C>G | NP_001272373.1:p.His698Gln | |
| NM_001285445.2:c.2091C>G | NP_001272374.1:p.His697Gln | |
| NM_001324019.2:c.2172C>G | NP_001310948.1:p.His724Gln | |
| NM_015027.4:c.2175C>G MANE Select | NP_055842.2:p.His725Gln | |
| NM_001285449.2:c.1399+6027C>G | NP_001272378.1:n.1399+6027C>G | |
| NM_001324020.2:c.1396+6027C>G | NP_001310949.1:n.1396+6027C>G | |
| NM_001324021.2:c.1318+6027C>G | NP_001310950.1:n.1318+6027C>G |